Device recall
Z-0492-2010: ADVANCE (R) CANAL FILLING STEM EXTENSION, REF: KSP1-0140, DIAMETER 11mm, LENGTH…
FDA device recall · Class III · Wright Medical Technology Inc
Key facts
| Recall number (Z-number) | Z-0492-2010 |
|---|---|
| Recall event | 53538 |
| Product | ADVANCE (R) CANAL FILLING STEM EXTENSION, REF: KSP1-0140, DIAMETER 11mm, LENGTH 140mm, 1 EACH, STERILE R, (FOR USE WITH CEMENT ONLY), SINGLE USE ONLY, (Ti6A14V), Wright Medical Technology, Inc., 5677 Airline Road, Arlington, TN 38002 |
| Product code | MBH |
| Recalling firm | Wright Medical Technology Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Dec 16, 2010 |
| 510(k) numbers | K061223 |
| FEI number | 1043534 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database